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Catalog Number:
40018
CAS Number:
330793-01-6
N- ( terc -butoxicarbonil)-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)anilina
Purity:
≥ 99 % (HPLC)
Synonym(s):
N -Boc-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)anilina, Pinacoléster del ácido 4-[( terc -butoxicarbonil)amino]fenilborónico, Éster de pinacol del ácido 4-(Boc-amino)fenilborónico, [4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)fenil]carbamato de terc -butilo
Documents
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Tamaño
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Product Information

N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilin is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is essential for the selective modification of amines in various chemical reactions. Its unique structure, incorporating a dioxaborolane moiety, enhances its reactivity and stability, making it an ideal candidate for applications in drug development and material science. Researchers often leverage this compound in the synthesis of complex organic molecules, particularly in the creation of pharmaceuticals where precise functional group manipulation is crucial.

The compound's ability to facilitate the formation of carbon-boron bonds opens up pathways for innovative synthetic strategies, particularly in the development of boron-containing compounds that are valuable in agrochemicals and advanced materials. Its stability under various reaction conditions and compatibility with a range of reagents make it a preferred choice for chemists looking to streamline their synthetic processes. With its robust performance and adaptability, this compound stands out as a key tool for researchers aiming to push the boundaries of chemical synthesis.

Synonyms
N -Boc-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)anilina, Pinacoléster del ácido 4-[( terc -butoxicarbonil)amino]fenilborónico, Éster de pinacol del ácido 4-(Boc-amino)fenilborónico, [4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)fenil]carbamato de terc -butilo
CAS Number
330793-01-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C17H26BNO4
Molecular Weight
319.21
MDL Number
MFCD02179439
PubChem ID
2734617
Melting Point
168 - 172 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
N -Boc-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)anilina, Pinacoléster del ácido 4-[( terc -butoxicarbonil)amino]fenilborónico, Éster de pinacol del ácido 4-(Boc-amino)fenilborónico, [4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)fenil]carbamato de terc -butilo
CAS Number
330793-01-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C17H26BNO4
Molecular Weight
319.21
MDL Number
MFCD02179439
PubChem ID
2734617
Melting Point
168 - 172 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilin is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of targeted therapies that require specific chemical modifications.
  • Organic Synthesis: It is employed in various organic synthesis reactions, acting as a protecting group for amines, which enhances the efficiency of multi-step synthetic pathways.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and coatings, which benefit from its unique chemical structure and properties.
  • Bioconjugation: Its ability to form stable bonds with biomolecules makes it valuable in bioconjugation applications, facilitating the development of biopharmaceuticals and diagnostic tools.
  • Research in Catalysis: This chemical is utilized in catalytic processes, where it can enhance reaction rates and selectivity, making it a crucial component in various catalytic systems.

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